@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP499722.RA_mzgtSp3gSr8RA74lcRfnSUS7D8Web-Hvdija2xElpQ
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP499722.RA_mzgtSp3gSr8RA74lcRfnSUS7D8Web-Hvdija2xElpQ130_head
{
this:
np:hasAssertion
dgn-np:NP499722.RA_mzgtSp3gSr8RA74lcRfnSUS7D8Web-Hvdija2xElpQ130_assertion
;
np:hasProvenance
dgn-np:NP499722.RA_mzgtSp3gSr8RA74lcRfnSUS7D8Web-Hvdija2xElpQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP499722.RA_mzgtSp3gSr8RA74lcRfnSUS7D8Web-Hvdija2xElpQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP499722.RA_mzgtSp3gSr8RA74lcRfnSUS7D8Web-Hvdija2xElpQ130_assertion
a
np:Assertion
.
dgn-np:NP499722.RA_mzgtSp3gSr8RA74lcRfnSUS7D8Web-Hvdija2xElpQ130_provenance
a
np:Provenance
.
dgn-np:NP499722.RA_mzgtSp3gSr8RA74lcRfnSUS7D8Web-Hvdija2xElpQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP499722.RA_mzgtSp3gSr8RA74lcRfnSUS7D8Web-Hvdija2xElpQ130_assertion
{
miriam-gene:1277
a
ncit:C16612
.
lld:C0029899
a
ncit:C7057
.
dgn-gda:DGN8a002d0de1ffa3b627f7be5c69a625e9
sio:SIO_000628
miriam-gene:1277
,
lld:C0029899
;
a
sio:SIO_001121
.
}
dgn-np:NP499722.RA_mzgtSp3gSr8RA74lcRfnSUS7D8Web-Hvdija2xElpQ130_provenance
{
dgn-np:NP499722.RA_mzgtSp3gSr8RA74lcRfnSUS7D8Web-Hvdija2xElpQ130_assertion
dcterms:description
"[Because of the clinical and histopathologic similarities between otosclerosis and type I osteogenesis imperfecta, we examined COL1A1 messenger RNA (mRNA) expression in cultured fibroblasts from patients with clinical otosclerosis to determine whether abnormalities of expression of COL1A1 were present, as has been reported in type I osteogenesis imperfecta.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:11860074
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP499722.RA_mzgtSp3gSr8RA74lcRfnSUS7D8Web-Hvdija2xElpQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}